Exosomes and other extracellular vesicles in HPV transmission and carcinogenesis

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Abstract

Extracellular vesicles (EVs), including exosomes (Exos), microvesicles (MVs) and apoptotic bodies (ABs) are released in biofluids by virtually all living cells. Tumor-derived Exos and MVs are garnering increasing attention because of their ability to participate in cellular communication or transfer of bioactive molecules (mRNAs, microRNAs, DNA and proteins) between neighboring cancerous or normal cells, and to contribute to human cancer progression. Malignant traits can also be transferred from apoptotic cancer cells to phagocytizing cells, either professional or non-professional. In this review, we focus on Exos and ABs and their relationship with human papillomavirus (HPV)-associated tumor development. The potential implication of EVs as theranostic biomarkers is also addressed.

Figures

  • Figure 1. Exoso e and icrovesicle biogenesis. Exoso es originate fro the in ard budding of endosomes to form multivesicular endosomes (MVEs). MVEs then fuse with the cell surface membrane to release exosomes into the extracellular medium. Some MVEs fuse with lysosomes. Microvesicles are produced by direct budding from the plasma membrane.
  • Figure 2. The four different modes of communication by exosomes and microvesicles. Extracellular vesicles serve as vehicles for cell-to-cell communication through horizontal transfer of bioactive molecules (proteins, lipids and nucleic acids). Extracellular vesicles (microvesicles (MVs) or exosomes (Exos)) produced from a secreting cell may be internalized by fusion (1), endocytosis (2), phagocytosis (3) or may interact with the membrane proteins of the target cell (4). Squares, triangles and circles represent membrane-associated proteins.

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CITATION STYLE

APA

Guenat, D., Hermetet, F., Prétet, J. L., & Mougin, C. (2017, August 7). Exosomes and other extracellular vesicles in HPV transmission and carcinogenesis. Viruses. MDPI AG. https://doi.org/10.3390/v9080211

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